(+-)(2R*,3S*)-2-Methyl-2-nitro-1,3-butanediol → (+-)(2R*,3S*)-2-amino-2-methyl-1,3-butanediol acetate
Reaction equation
[C:1]([OH:4])(=[O:3])[CH3:2].[NH2:5][C@@:6]([CH3:12])([C@H:9]([OH:11])[CH3:10])[CH2:7][OH:8].C[C@]([N+]([O-])=O)([C@@H](O)C)CO>>[C:1]([OH:4])(=[O:3])[CH3:2].[NH2:5][C@@:6]([CH3:12])([C@@H:9]([OH:11])[CH3:10])[CH2:7][OH:8]Participants
3
Procedure
Using the procedure described for 30E (+-)(2R*,3S*)-2-methyl-2-nitro-1,3-butanediol (30A) gave (+-)(2R*,3S*)-2-amino-2-methyl-1,3-butanediol acetate (93%) mp 163°-165° (C, H, N).
Sources & evidence
- ORD record
- ord-f05c3fc9c6484445b4d4a46be2dcfccf
- Source dataset
- uspto-grants-1988_01
- Patent number
- US04719049
Reaction notes
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